F. Ghezzi et al., ELEVATED INTERLEUKIN-8 CONCENTRATIONS IN AMNIOTIC-FLUID OF MOTHERS WHOSE NEONATES SUBSEQUENTLY DEVELOP BRONCHOPULMONARY DYSPLASIA, European journal of obstetrics, gynecology, and reproductive biology, 78(1), 1998, pp. 5-10
Objective: To determine if an intrauterine sub-clinical inflammatory p
rocess is a risk factor for the development of bronchopulmonary dyspla
sia. Methods: A cohort study was conducted in patients who met the fol
lowing criteria: (1) Singleton gestation; (2) preterm labor or preterm
premature rupture of the membranes, (3) amniocentesis for microbiolog
ic studies of the amniotic fluid and (41 delivery between 24 and 28 we
eks of gestation. Bronchopulmonary dysplasia was defined as the need f
or supplemental oxygen fur 78 days or longer after birth, associated w
ith compatible chest radiographic findings. Amniotic fluid interleukin
-8, was measured using a specific immunoassay. Logistic regression ana
lysis and bootstrap procedure were used for statistical purposes. Resu
lts: Forty-seven patients met the inclusion criteria for this study. A
mong these patients, the prevalence of bronchopulmonary dysplasia was
23.4% (11/47). Amniotic fluid culture was positive in 21 out of 47 (44
.7%) patients. Median (range) amniotic fluid interleukin-8 concentrati
on was higher in patients whose neonates subsequently developed bronch
opulmonary dysplasia than in those who did not (17 [9.8-583.7] ng ml(-
1) versus 9.6 [0.91-744] ng ml(-1), P = 0.057). An amniotic fluid IL-8
level greater than 11.5 ng ml(-1) was far more common in mothers whos
e fetuses went on to develop bronchopulmonary dysplasia than in those
who did not (10/11 [90.9%] versus 17/36 [47%]; P = 0.01). This relatio
nship remained significant even after correcting for the effect of ges
tational age and birthweight (Odds ratio: 11.9; P < 0.05), Conclusion:
Sub-clinical intrauterine inflammation is a risk factor for the subse
quent development of bronchopulmonary dysplasia. We propose that in ut
ero aspiration of fluid with high concentration of pro-inflammatory me
diators may contribute to the lune injury responsible for the developm
ent of bronchopulmonary dysplasia. (C) 1998 Elsevier Science ireland L
td.